• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

[17,20-Desmolase deficiency].

作者信息

Yanase T, Nawata H

机构信息

Third Department of Internal Medicine, Faculty of Medicine, Kyushu University.

出版信息

Ryoikibetsu Shokogun Shirizu. 1993(1):911-4.

PMID:7757785
Abstract
摘要

相似文献

1
[17,20-Desmolase deficiency].[17,20-脱氨酶缺乏症]
Ryoikibetsu Shokogun Shirizu. 1993(1):911-4.
2
[A case of male pseudohermaphroditism due to 17,20-desmolase deficiency].[一例因17,20-裂解酶缺乏导致的男性假两性畸形病例]
Nihon Sanka Fujinka Gakkai Zasshi. 1988 Feb;40(2):259-62.
3
Prismatic cases: 17,20-desmolase (17,20-lyase) deficiency.棱柱状病例：17,20-碳链裂解酶（17,20-裂解酶）缺乏症。
J Clin Endocrinol Metab. 1996 Feb;81(2):457-9. doi: 10.1210/jcem.81.2.8636249.
4
Conversion from pure 17,20-desmolase- to combined 17,20-desmolase/17 alpha-hydroxylase deficiency with age.随着年龄增长，从单纯的17,20-碳链裂解酶缺乏转变为17,20-碳链裂解酶/17α-羟化酶联合缺乏。
Acta Endocrinol (Copenh). 1992 Aug;127(2):97-9. doi: 10.1530/acta.0.1270097.
5
17 alpha-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition.17α-羟化酶/17,20-裂解酶缺乏症：从临床研究到分子定义
Endocr Rev. 1991 Feb;12(1):91-108. doi: 10.1210/edrv-12-1-91.
6
Combined 17-hydroxylase and 17,20-desmolase deficiencies: evidence for synthesis of a defective cytochrome P450c17.17-羟化酶和17,20-裂解酶联合缺乏症：合成缺陷型细胞色素P450c17的证据
J Clin Endocrinol Metab. 1989 Feb;68(2):309-16. doi: 10.1210/jcem-68-2-309.
7
Endocrine findings in male pseudohermaphroditism.男性假两性畸形的内分泌学表现
Eur J Pediatr. 1993;152 Suppl 2:S58-61. doi: 10.1007/BF02125441.
8
Incomplete virilization and subclinical mineralocorticoid excess in a boy with partial 17,20-desmolase/17 alpha-hydroxylase deficiency.
Acta Endocrinol (Copenh). 1990 Feb;122(2):263-6. doi: 10.1530/acta.0.1220263.
9
Marked attenuation of ultradian and circadian rhythms of dehydroepiandrosterone in postmenopausal women: evidence for a reduced 17,20-desmolase enzymatic activity.绝经后女性脱氢表雄酮的超日节律和昼夜节律显著减弱：17,20-裂解酶活性降低的证据。
J Clin Endocrinol Metab. 1990 Oct;71(4):900-6. doi: 10.1210/jcem-71-4-900.
10
Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency.正常和突变型人甾体17α-羟化酶基因的结构特征：17α-羟化酶/17,20裂解酶联合缺乏症一个实例的分子基础
Mol Endocrinol. 1988 Jun;2(6):564-70. doi: 10.1210/mend-2-6-564.